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22. [Trisomy 21 in a boy with progressive muscular dystrophy (Duchenne)]. Moser H Z Kinderheilkd; 1971; 109(4):318-25. PubMed ID: 4252123 [No Abstract] [Full Text] [Related]
23. Clinical symptoms in a female carrier of Duchenne muscular dystrophy. Zatz M; Levisky RB; Levy JA; Valente BO; Gianotti M; Frota-Pessoa O J Genet Hum; 1973 Dec; 21(4):297-305. PubMed ID: 4792239 [No Abstract] [Full Text] [Related]
24. Genetic counselling in neuromuscular diseases in Western Australia. Hurse PV; Kakulas BA Proc Aust Assoc Neurol; 1974; 11():145-53. PubMed ID: 4469625 [No Abstract] [Full Text] [Related]
25. [On Becker's benign muscular dystrophy: study of a family with 10 affected members in 6 generations]. Caruso G; Campanella G Acta Neurol (Napoli); 1968; 23(4):709-31. PubMed ID: 5747395 [No Abstract] [Full Text] [Related]
26. Ultrastructure of skeletal muscle in muscular dystrophy, the carrier state and other human myopathies. Papadimitriou JM; Kakulas BA Proc Aust Assoc Neurol; 1968; 5(1):87-94. PubMed ID: 5250033 [No Abstract] [Full Text] [Related]
27. X-linked muscular dystrophy, benign form with contractures. McKusick VA Birth Defects Orig Artic Ser; 1971 Feb; 7(2):113-5. PubMed ID: 5173119 [No Abstract] [Full Text] [Related]
28. Study of the central nervous system in Duchenne type of muscular dystrophy. Desai AD; Jayam AV; Banerji AP; Kohiyar FN; Ardhapurkar I Neurol India; 1969 Dec; 17(4):184-90. PubMed ID: 5367415 [No Abstract] [Full Text] [Related]
29. Studies of the carrier state in the Duchenne type of muscular dystrophy. 2. Quantitative electromyography as a method of carrier detection. Gardner-Medwin D J Neurol Neurosurg Psychiatry; 1968 Apr; 31(2):124-34. PubMed ID: 5684019 [No Abstract] [Full Text] [Related]
30. The significance of changes in the blood serum electrolytes in the detection of heterozygous carriers of Duchenne myopathy. Grinio LP Sov Genet; 1974 Mar; 7(12):1596-9. PubMed ID: 4827770 [No Abstract] [Full Text] [Related]
37. The incidence of Duchenne muscular dystrophy in eastern Austria. The controversy regarding CK screening. Hauser E; Toifl K; Mad A; Bittner R Wien Klin Wochenschr; 1993; 105(15):433-6. PubMed ID: 8104369 [TBL] [Abstract][Full Text] [Related]
38. Harmonic analysis in carriers of Duchenne muscular dystrophy. Gersten JW; Stillwell DM; Rose NA Arch Phys Med Rehabil; 1967 Apr; 48(4):164-9. PubMed ID: 6022539 [No Abstract] [Full Text] [Related]
39. Duchenne muscular dystrophy: does serum myoglobin correlate with serum creatine kinase? Kiessling WR; Beckmann R Muscle Nerve; 1981; 4(3):257. PubMed ID: 7242564 [No Abstract] [Full Text] [Related]
40. Further studies concerning the detection of carriership in the Duchenne type of dystrophy. Hausmanowa-Petrusewicz I; Prot J; Dobosz I; Emeryk B; Rowińska K; Rubach K; Kopeć A; Kopeć J Eur Neurol; 1971; 5(3):186-96. PubMed ID: 5117629 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]